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Methyl (Z)-oct-4-enoate, also known as methyl (4Z)-oct-4-enoate, is an organic compound that belongs to the class of esters. It is characterized by the presence of a carbon-carbon double bond in the Z configuration, which gives it unique chemical and physical properties. methyl (Z)-oct-4-enoate can be synthesized from cis-4-octenoic acid ethyl ester and methanol in the presence of a sodium catalyst. Methyl (Z)-oct-4-enoate is known for its distinct chemical structure and potential applications in various industries.

21063-71-8

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21063-71-8 Usage

Uses

Used in Flavor and Fragrance Industry:
Methyl (Z)-oct-4-enoate is used as a flavoring agent for its fruity and tropical aroma. It is commonly employed in the creation of artificial fruit flavors, particularly those mimicking the taste of pineapple, starfruit, and pawpaw. The compound's unique scent profile makes it a valuable addition to the flavor and fragrance industry.
Used in Chemical Synthesis:
Methyl (Z)-oct-4-enoate serves as a versatile building block in organic synthesis, allowing for the development of various chemical compounds with diverse applications. Its carbon-carbon double bond can be selectively functionalized, making it a useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
Due to its unique chemical structure, methyl (Z)-oct-4-enoate is often utilized in research and development for studying various chemical reactions and processes. It can be employed as a model compound to investigate the reactivity of carbon-carbon double bonds, as well as to explore new synthetic routes and methodologies.
Used in Analytical Chemistry:
Methyl (Z)-oct-4-enoate can be used as a reference compound in analytical chemistry for the calibration of instruments and the development of new analytical methods. Its distinct chemical properties make it suitable for testing the performance of chromatographic techniques, spectroscopic methods, and other analytical tools.

Preparation

From cis-4-octenoic acid ethyl ester and methanol in the presence of sodium catalyst.

Check Digit Verification of cas no

The CAS Registry Mumber 21063-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21063-71:
(7*2)+(6*1)+(5*0)+(4*6)+(3*3)+(2*7)+(1*1)=68
68 % 10 = 8
So 21063-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-3-4-5-6-7-8-9(10)11-2/h5-6H,3-4,7-8H2,1-2H3

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